Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
T |
C |
15: 81,946,852 (GRCm39) |
S250P |
probably benign |
Het |
Ahcyl1 |
T |
A |
3: 107,578,494 (GRCm39) |
I248F |
possibly damaging |
Het |
Alpk2 |
T |
A |
18: 65,482,646 (GRCm39) |
E454V |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,829,070 (GRCm39) |
T2580S |
|
Het |
Anks1 |
G |
A |
17: 28,128,571 (GRCm39) |
G46R |
possibly damaging |
Het |
Arhgap45 |
A |
G |
10: 79,857,635 (GRCm39) |
E322G |
probably damaging |
Het |
Arhgef2 |
T |
C |
3: 88,528,576 (GRCm39) |
I4T |
probably benign |
Het |
C1qtnf4 |
T |
C |
2: 90,720,351 (GRCm39) |
I208T |
probably damaging |
Het |
Cachd1 |
T |
A |
4: 100,832,092 (GRCm39) |
N751K |
probably benign |
Het |
Cacna1a |
G |
T |
8: 85,320,808 (GRCm39) |
V1589F |
possibly damaging |
Het |
Cacnb1 |
T |
C |
11: 97,902,197 (GRCm39) |
H205R |
probably benign |
Het |
Castor1 |
A |
G |
11: 4,169,015 (GRCm39) |
K61E |
probably benign |
Het |
Ccdc9b |
G |
T |
2: 118,591,077 (GRCm39) |
A152E |
probably benign |
Het |
Clvs2 |
C |
A |
10: 33,389,307 (GRCm39) |
R311L |
probably benign |
Het |
Crim1 |
G |
T |
17: 78,610,504 (GRCm39) |
G320* |
probably null |
Het |
Crtam |
A |
T |
9: 40,895,671 (GRCm39) |
D218E |
probably benign |
Het |
Cwc27 |
G |
A |
13: 104,943,158 (GRCm39) |
T128I |
probably damaging |
Het |
Cyp4a14 |
T |
A |
4: 115,349,347 (GRCm39) |
I238F |
probably benign |
Het |
D930020B18Rik |
A |
C |
10: 121,503,563 (GRCm39) |
E246A |
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,410,044 (GRCm39) |
V504E |
probably benign |
Het |
Enpp6 |
T |
A |
8: 47,518,948 (GRCm39) |
S239T |
probably damaging |
Het |
Eri2 |
A |
T |
7: 119,384,824 (GRCm39) |
I559N |
probably benign |
Het |
Fbxo34 |
T |
C |
14: 47,768,724 (GRCm39) |
Y746H |
probably damaging |
Het |
Galr1 |
A |
T |
18: 82,424,103 (GRCm39) |
L58Q |
probably damaging |
Het |
Ghdc |
A |
G |
11: 100,658,863 (GRCm39) |
V423A |
probably benign |
Het |
Glt28d2 |
T |
C |
3: 85,779,059 (GRCm39) |
D138G |
probably benign |
Het |
Gm266 |
A |
T |
12: 111,451,763 (GRCm39) |
C148S |
probably benign |
Het |
Gnas |
C |
T |
2: 174,141,132 (GRCm39) |
T493M |
unknown |
Het |
Hivep2 |
T |
C |
10: 14,015,203 (GRCm39) |
I1790T |
probably damaging |
Het |
Impg1 |
A |
G |
9: 80,287,276 (GRCm39) |
V390A |
probably benign |
Het |
Isy1 |
A |
G |
6: 87,796,574 (GRCm39) |
F239L |
possibly damaging |
Het |
Itgb5 |
A |
G |
16: 33,685,917 (GRCm39) |
T86A |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,382,481 (GRCm39) |
C1458R |
possibly damaging |
Het |
Krt28 |
T |
C |
11: 99,255,921 (GRCm39) |
E446G |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,129,404 (GRCm39) |
Q3071L |
|
Het |
Lasp1 |
A |
G |
11: 97,697,593 (GRCm39) |
|
probably benign |
Het |
Lmf2 |
T |
C |
15: 89,237,419 (GRCm39) |
K348E |
probably benign |
Het |
Lrch3 |
G |
T |
16: 32,796,108 (GRCm39) |
E331* |
probably null |
Het |
Lzic |
T |
A |
4: 149,573,141 (GRCm39) |
F98I |
probably damaging |
Het |
Map7d1 |
C |
A |
4: 126,127,440 (GRCm39) |
|
probably null |
Het |
Marchf8 |
C |
T |
6: 116,378,405 (GRCm39) |
T113I |
possibly damaging |
Het |
Mgrn1 |
A |
T |
16: 4,745,740 (GRCm39) |
K423* |
probably null |
Het |
Muc20 |
G |
A |
16: 32,615,266 (GRCm39) |
T37I |
possibly damaging |
Het |
Myh15 |
A |
G |
16: 48,959,044 (GRCm39) |
E972G |
probably damaging |
Het |
Myocd |
T |
A |
11: 65,087,167 (GRCm39) |
K253N |
probably damaging |
Het |
Myod1 |
T |
G |
7: 46,026,575 (GRCm39) |
L160R |
probably damaging |
Het |
Nanog |
T |
C |
6: 122,684,799 (GRCm39) |
S20P |
probably benign |
Het |
Nat8f2 |
A |
T |
6: 85,844,683 (GRCm39) |
Y226* |
probably null |
Het |
Nsmf |
A |
G |
2: 24,949,077 (GRCm39) |
K277R |
probably null |
Het |
Nsrp1 |
C |
T |
11: 76,967,503 (GRCm39) |
G30R |
probably damaging |
Het |
Nsun6 |
C |
A |
2: 15,003,009 (GRCm39) |
R389L |
probably benign |
Het |
Obscn |
G |
A |
11: 58,943,397 (GRCm39) |
R4251C |
probably benign |
Het |
Or10g9 |
A |
T |
9: 39,912,172 (GRCm39) |
M117K |
probably damaging |
Het |
Or11h4 |
C |
T |
14: 50,974,199 (GRCm39) |
C140Y |
probably benign |
Het |
Or51h1 |
A |
G |
7: 102,308,441 (GRCm39) |
T138A |
probably damaging |
Het |
Or5w20 |
G |
A |
2: 87,726,902 (GRCm39) |
D120N |
probably damaging |
Het |
Pgm1 |
T |
C |
4: 99,843,918 (GRCm39) |
L567P |
probably damaging |
Het |
Polrmt |
G |
T |
10: 79,576,535 (GRCm39) |
H474N |
probably benign |
Het |
Ppfia2 |
A |
G |
10: 106,664,885 (GRCm39) |
I374V |
probably benign |
Het |
Pramel5 |
T |
A |
4: 143,999,545 (GRCm39) |
I181F |
probably benign |
Het |
Prpf4b |
T |
A |
13: 35,083,870 (GRCm39) |
Y880N |
probably damaging |
Het |
Ptpn3 |
G |
A |
4: 57,249,957 (GRCm39) |
Q180* |
probably null |
Het |
Ptprc |
T |
C |
1: 138,008,627 (GRCm39) |
R687G |
probably damaging |
Het |
Rnaseh2a |
T |
C |
8: 85,684,638 (GRCm39) |
T241A |
probably damaging |
Het |
Rnf148 |
T |
A |
6: 23,654,802 (GRCm39) |
I65F |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,831 (GRCm39) |
I2348V |
|
Het |
Rttn |
A |
G |
18: 89,035,334 (GRCm39) |
N736S |
possibly damaging |
Het |
Ryr3 |
A |
C |
2: 112,633,534 (GRCm39) |
V2093G |
probably damaging |
Het |
Selenof |
T |
A |
3: 144,283,370 (GRCm39) |
F33L |
probably benign |
Het |
Sh2d3c |
C |
T |
2: 32,635,889 (GRCm39) |
R238* |
probably null |
Het |
Slc23a4 |
T |
C |
6: 34,923,235 (GRCm39) |
K543R |
probably benign |
Het |
Smn1 |
A |
T |
13: 100,272,210 (GRCm39) |
N278I |
possibly damaging |
Het |
Sox7 |
G |
A |
14: 64,185,509 (GRCm39) |
A182T |
probably benign |
Het |
Spata31e5 |
T |
A |
1: 28,817,120 (GRCm39) |
Y304F |
probably benign |
Het |
Sptlc2 |
A |
T |
12: 87,359,533 (GRCm39) |
I501N |
probably benign |
Het |
Srf |
T |
C |
17: 46,866,271 (GRCm39) |
T162A |
probably benign |
Het |
Srm |
C |
T |
4: 148,676,039 (GRCm39) |
|
probably benign |
Het |
Stim1 |
CAGCGCCTGACGGAGC |
CAGC |
7: 102,080,118 (GRCm39) |
|
probably benign |
Het |
Taar8a |
T |
C |
10: 23,952,714 (GRCm39) |
L106P |
probably damaging |
Het |
Tcte1 |
A |
G |
17: 45,850,798 (GRCm39) |
H358R |
possibly damaging |
Het |
Tmem205 |
A |
G |
9: 21,837,587 (GRCm39) |
S20P |
probably damaging |
Het |
Trav16 |
T |
A |
14: 53,980,910 (GRCm39) |
V33E |
possibly damaging |
Het |
Trmt2a |
C |
T |
16: 18,070,041 (GRCm39) |
Q419* |
probably null |
Het |
Ttc19 |
A |
G |
11: 62,203,997 (GRCm39) |
I319M |
probably benign |
Het |
Txndc16 |
T |
C |
14: 45,400,467 (GRCm39) |
I345V |
probably benign |
Het |
Ube3b |
T |
C |
5: 114,553,370 (GRCm39) |
I914T |
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,727,957 (GRCm39) |
F107L |
possibly damaging |
Het |
Vmn1r73 |
T |
C |
7: 11,490,407 (GRCm39) |
F75S |
possibly damaging |
Het |
Vmn2r54 |
A |
T |
7: 12,363,753 (GRCm39) |
M380K |
possibly damaging |
Het |
Wdr7 |
T |
A |
18: 63,927,317 (GRCm39) |
M989K |
possibly damaging |
Het |
Zcchc3 |
A |
G |
2: 152,256,385 (GRCm39) |
S105P |
probably benign |
Het |
Zfp735 |
T |
A |
11: 73,601,806 (GRCm39) |
V250E |
possibly damaging |
Het |
|
Other mutations in Trf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Trf
|
APN |
9 |
103,098,156 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00424:Trf
|
APN |
9 |
103,104,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00793:Trf
|
APN |
9 |
103,103,342 (GRCm39) |
unclassified |
probably benign |
|
IGL01139:Trf
|
APN |
9 |
103,100,803 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01658:Trf
|
APN |
9 |
103,104,055 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02671:Trf
|
APN |
9 |
103,089,181 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02996:Trf
|
APN |
9 |
103,098,102 (GRCm39) |
missense |
probably benign |
0.01 |
R0060:Trf
|
UTSW |
9 |
103,098,121 (GRCm39) |
missense |
probably benign |
0.11 |
R0060:Trf
|
UTSW |
9 |
103,098,121 (GRCm39) |
missense |
probably benign |
0.11 |
R0096:Trf
|
UTSW |
9 |
103,099,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Trf
|
UTSW |
9 |
103,099,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R0112:Trf
|
UTSW |
9 |
103,104,155 (GRCm39) |
unclassified |
probably benign |
|
R0234:Trf
|
UTSW |
9 |
103,104,078 (GRCm39) |
splice site |
probably null |
|
R0234:Trf
|
UTSW |
9 |
103,104,078 (GRCm39) |
splice site |
probably null |
|
R0411:Trf
|
UTSW |
9 |
103,094,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R0456:Trf
|
UTSW |
9 |
103,104,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Trf
|
UTSW |
9 |
103,100,132 (GRCm39) |
critical splice donor site |
probably null |
|
R1419:Trf
|
UTSW |
9 |
103,103,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Trf
|
UTSW |
9 |
103,102,335 (GRCm39) |
splice site |
probably null |
|
R3943:Trf
|
UTSW |
9 |
103,100,151 (GRCm39) |
missense |
probably benign |
0.00 |
R4431:Trf
|
UTSW |
9 |
103,089,075 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4609:Trf
|
UTSW |
9 |
103,089,184 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4658:Trf
|
UTSW |
9 |
103,100,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R4830:Trf
|
UTSW |
9 |
103,105,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R4925:Trf
|
UTSW |
9 |
103,096,445 (GRCm39) |
missense |
probably benign |
0.00 |
R4929:Trf
|
UTSW |
9 |
103,105,074 (GRCm39) |
intron |
probably benign |
|
R4931:Trf
|
UTSW |
9 |
103,105,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R5139:Trf
|
UTSW |
9 |
103,100,133 (GRCm39) |
critical splice donor site |
probably null |
|
R5272:Trf
|
UTSW |
9 |
103,105,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R5692:Trf
|
UTSW |
9 |
103,103,324 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6227:Trf
|
UTSW |
9 |
103,107,504 (GRCm39) |
start gained |
probably benign |
|
R6365:Trf
|
UTSW |
9 |
103,099,327 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6928:Trf
|
UTSW |
9 |
103,099,307 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7127:Trf
|
UTSW |
9 |
103,102,326 (GRCm39) |
missense |
probably benign |
|
R7231:Trf
|
UTSW |
9 |
103,102,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R7648:Trf
|
UTSW |
9 |
103,105,168 (GRCm39) |
missense |
probably benign |
0.01 |
R8088:Trf
|
UTSW |
9 |
103,089,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R8095:Trf
|
UTSW |
9 |
103,087,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R8317:Trf
|
UTSW |
9 |
103,094,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R8443:Trf
|
UTSW |
9 |
103,094,675 (GRCm39) |
missense |
probably damaging |
0.98 |
R8735:Trf
|
UTSW |
9 |
103,087,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R8854:Trf
|
UTSW |
9 |
103,107,529 (GRCm39) |
unclassified |
probably benign |
|
R9131:Trf
|
UTSW |
9 |
103,089,087 (GRCm39) |
missense |
probably damaging |
0.99 |
R9360:Trf
|
UTSW |
9 |
103,094,734 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9499:Trf
|
UTSW |
9 |
103,099,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9526:Trf
|
UTSW |
9 |
103,104,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9551:Trf
|
UTSW |
9 |
103,099,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9552:Trf
|
UTSW |
9 |
103,099,283 (GRCm39) |
missense |
probably benign |
0.00 |
|